A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574642



Internal ID16362051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27164515..27209614hg38UCSC Ensembl
Innerchr17:25491541..25536640hg19UCSC Ensembl
Innerchr17:22515668..22560767hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3845100
hg1945100
hg1845100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5512n54
Supporting Variantsnssv868984
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574642
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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